Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Naoki Uchisaka"'
Autor:
Hiroshi Kishimoto, Motohiro Kato, Shoji Watanabe, Koichi Oshima, Ryoji Hanada, Yoshihiro Gocho, Ayumu Arakawa, Naoko Yasui, Katsuyoshi Koh, Masafumi Seki, Akira Kikuchi, Daisuke Tomizawa, Naoki Uchisaka, Myoung-ja Park, Eiji Oguma
Publikováno v:
Journal of Pediatric Hematology/Oncology. 35:554-558
Background Kasabach-Merritt phenomenon (KMP) is a rare condition and optimal treatments have not yet been established, especially for cases that are unresponsive to first-line therapy. We retrospectively reviewed 11 KMP cases treated over the past 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2354e733a38b5687871fd36c90e48abf
https://doi.org/10.1097/mph.0b013e318281558e
https://doi.org/10.1097/mph.0b013e318281558e
Autor:
Tomohiro Morio, Naoki Uchisaka, Masatoshi Takagi, Daiju Oba, Shin-ichiro Hamano, Masaharu Hayashi, Motoyuki Minamitani, Shuki Mizutani, Hiroshi Kishimoto, Akira Kikuchi
Publikováno v:
Acta Neuropathologica. 119:513-520
Ataxia-telangiectasia-like disorder (ATLD) is caused by mutations of the MRE11 gene and is characterized by cerebellar ataxia, increased frequency of chromosomal translocations and hypersensitivity to ionizing radiation. ATLD is a rare genetic diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50cba93cfde31bf4b2e655fb6070ca48
https://doi.org/10.1007/s00401-010-0639-4
https://doi.org/10.1007/s00401-010-0639-4
Autor:
Tomohiro Morio, Osamu Ohara, Ryoji Hanada, Shigeaki Nonoyama, Naomi Takahashi, Naoki Uchisaka, Fumiaki Watanabe, Shuki Mizutani, Shinji Mochizuki, Masaki Sato, Akira Kikuchi, Kohsuke Imai
Publikováno v:
The Journal of pediatrics. 155(3)
We report on 2 brothers with ataxia-telangiectasia-like disorder with lung adenocarcinoma. They both had ataxia with cerebellar atrophy and mental retardation. They had the same mutation of the MRE11 gene, which has not been reported previously (c.72
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71bb90453801e72eba05fc042065f973
https://pubmed.ncbi.nlm.nih.gov/19732584
https://pubmed.ncbi.nlm.nih.gov/19732584
Autor:
Naoki Uchisaka, Ryoji Hanada, Akira Kikuchi, Koichi Oshima, Miharu Yabe, Shinji Mochizuki, Daisuke Toyama
Publikováno v:
International Journal of Hematology. 89:722-723
The most important clinical features of Fanconi anemia (FA) are hematologic disorders and these are responsible for high incidence of morbidity and mortality. During birth, the blood count is usually normal and macrocytosis is often the first detecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eef48f14e39c8a5ed62d7d8263c077f6
https://doi.org/10.1007/s12185-009-0329-y
https://doi.org/10.1007/s12185-009-0329-y